{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Portland",
      "address_1": "825 NE 25th Ave",
      "reason_for_recall": "Riverpoint Medical is recalling PGLA Surgical Suture (Vilet) because the label indicates the suture is undyed and it is actually a violet colored suture.",
      "address_2": "",
      "product_quantity": "1932 pieces",
      "code_info": "Lot 120716-01",
      "center_classification_date": "20131118",
      "distribution_pattern": "US Distribution in the states of: AZ, FL, and TX.",
      "state": "OR",
      "product_description": "Polyglycolic-Lactic Acid Absorbable Surgical Suture    Label reads in part \"Coated VILET *** (Polyglacin 910) Suture UNDYED BRANDED V423 *** Riverpoint ***\"    PGLA surgical suture is indicated for use in general soft tissue approximation and/or ligation, including use in opthalmic procedures, but not for use in cardiovascular and neurological tissues",
      "report_date": "20131127",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Riverpoint Medical, LLC",
      "recall_number": "Z-0347-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65584",
      "termination_date": "20131121",
      "more_code_info": "",
      "recall_initiation_date": "20121213",
      "postal_code": "97232-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}